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| | 2,4,5-TRICHLOROBENZENESULFONYL CHLORIDE Basic information |
| Product Name: | 2,4,5-TRICHLOROBENZENESULFONYL CHLORIDE | | Synonyms: | AKOS 213-16;2,4,5-TRICHLOROBENZENE-1-SULFONYL CHLORIDE;2,4,5-TRICHLOROBENZENESULFONYL CHLORIDE;2,4,5-TRICHLOROBENZENESULPHONYL CHLORIDE;2,4,5-Trichlorobenzenesulfonyl chloride, GC 97%;2,4,5-THRICHLOROBENZENESULFONYL CHLORIDE;2,4,5-TRICHLOROBENZENESULFONYL CHLORIDE 98+%;2,4,5-trichloro-benzenesulfonylchlorid | | CAS: | 15945-07-0 | | MF: | C6H2Cl4O2S | | MW: | 279.96 | | EINECS: | 240-079-0 | | Product Categories: | Sulfonyl Halides;Sulfur Compounds;Benzenesulfonyl chloride;Organic Building Blocks | | Mol File: | 15945-07-0.mol |  |
| | 2,4,5-TRICHLOROBENZENESULFONYL CHLORIDE Chemical Properties |
| Melting point | 65-69 °C | | Boiling point | 138 °C(Press: 0.5 Torr) | | density | 1.728±0.06 g/cm3(Predicted) | | storage temp. | Inert atmosphere,2-8°C | | solubility | soluble in Toluene | | form | powder to crystal | | color | White to Almost white | | Sensitive | Moisture Sensitive | | BRN | 1112595 | | InChI | 1S/C6H2Cl4O2S/c7-3-1-5(9)6(2-4(3)8)13(10,11)12/h1-2H | | InChIKey | WNVVRCKTQSCPAC-UHFFFAOYSA-N | | SMILES | Clc1cc(Cl)c(cc1Cl)S(Cl)(=O)=O | | CAS DataBase Reference | 15945-07-0(CAS DataBase Reference) | | EPA Substance Registry System | Benzenesulfonyl chloride, 2,4,5-trichloro- (15945-07-0) |
| Hazard Codes | C | | Risk Statements | 34-14 | | Safety Statements | 26-27-36/37/39-8-45 | | RIDADR | 3261 | | WGK Germany | 3 | | Hazard Note | Corrosive/Moisture Sensitive | | TSCA | TSCA listed | | HazardClass | 8 | | PackingGroup | II | | HS Code | 29049095 | | Storage Class | 8A - Combustible corrosive hazardous materials | | Hazard Classifications | Skin Corr. 1B |
| Provider | Language |
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ALFA
| English |
| | 2,4,5-TRICHLOROBENZENESULFONYL CHLORIDE Usage And Synthesis |
| Chemical Properties | White or cream solid | | Uses | 2,4,5-Trichloro-benzenesulfonyl chloride is a useful building block for organic synthesis. | | Production Methods | 2,4,5-TrichlorobenzenesulfonylChloride is obtained from trichlorobenzene by chlorosulfonation with chlorosulfuric acid at 90 ℃ and pouring the reaction mass into water. | | Application | Esters and amides of several chlorobenzenesulfonic acids (particularly 4-chlorobenzenesulfonic acid, 2,5-dichlorobenzenesulfonic acid, and 2,4,5-trichlorobenzenesulfonic acid) have acquired some importance as crop protection products and agents for the control of fiber pests.
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| | 2,4,5-TRICHLOROBENZENESULFONYL CHLORIDE Preparation Products And Raw materials |
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